ClearanceBrief
510(k) K843719 ยท DYB Introducer, Catheter

SINGLE WALL INTRODUCER NEEDLE

ApplicantOcean Medical Products, Ltd., Wyoming MI, US
DecisionSubstantially Equivalent, Oct 18, 1984
ReceivedSep 24, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843719

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.